Essentiality of dietary cholesterol and its interactions with phospholipid in juvenile slipper lobster (Thenus australiensis)

This study was conducted to verify the essentiality of dietary cholesterol for early juvenile slipper lobster, Thenus australiensis (initial weight 4.50 ± 0.72 g, mean ± SD, CV = 0.16), and to explore the potential for interactions between dietary cholesterol and phospholipid. An 8-week experiment was conducted using six experimental feeds containing three supplemental cholesterol concentrations (0, 0.2 and 0.4% dry matter) at two supplemental phospholipid concentrations (0% and 1.0% dry matter). Dietary cholesterol concentrations of ≥ 0.2% resulted in up to threefold greater weight gain compared to 0% dietary cholesterol, but without any significant main or interactive dietary phospholipid effect. An interaction was observed for lobster survival with lowest survival (46%) recorded for combined 0% cholesterol and 0% phospholipid compared to every other treatment (71–100%). However, all surviving lobsters at 0% dietary cholesterol, regardless of dietary phospholipid level, were in poor nutritional condition. Apparent feed intake (AFI) was significantly higher at dietary cholesterol ≥ 0.2% but was lower for each corresponding dietary cholesterol level at 1% dietary phospholipid. This implied that the feed conversion ratio was improved with supplemental phospholipid. In conclusion, this study confirms the essential nature of dietary cholesterol and that dietary phospholipid can provide additional benefits.


Discussion
Cholesterol is considered an essential nutrient for decapod crustaceans, although the quantitative dietary requirements have been shown to vary for different species, developmental stages, life histories and in combination with other key nutrients 3 .Despite possessing key attributes desirable for experimentation and captive rearing 30,31 , slipper lobsters (Scyllaridae) remain a critically understudied decapod family.Consequently, little is known regarding the nutritional requirements of the slipper lobster, T. australiensis.While recent studies have started to explore their nutritional requirements and physiology in more detail 28,30,32,33 , the present study is the first to examine the importance of dietary Chol.For several crustacean species other than the slipper lobsters, there are some evidence that dietary PhosL may spare Chol 3 .Thus, in the present study, such interactive effects were Table 1.Wet weight, dry weight and general growth performance parameters (mean ± SEM, n = 3) of juvenile Thenus australiensis at three cholesterol (Chol %) and two phospholipid (PhosL %) supplemental dietary concentrations after 8 weeks.P value in bold indicate statistically significant difference (P < 0.05). .Where a statistical main effect (Chol and PhosL) or interaction (Chol*PhosL) was observed, superscripts are used to denote homogenous data ranges (P > 0.05) for treatment means determined by Tukey's posthoc analysis.n.s.= not significant.WG = weight gain; BWG = body weight gain; SGR = specific growth rate; HPSI = hepatosomatic index; AFI = apparent feed intake; DM = dry matter; FCR = feed conversion ratio.investigated.It was found that provision of sufficient dietary Chol (between 0.05 and 0.2% DM in feed) is essential for normal moulting and growth.Cholesterol was the sole factor linked to significant differences in growth and general nutritional condition (whole-body) at dietary Chol levels ≥ 0.2% DM, while 1% DM dietary PhosL had significant effects on AFI and FCR resulting in improved feed efficiency.Furthermore, an interactive effect between dietary Chol and PhosL was found for lobster survival, primarily whereby inclusion of dietary PhosL significantly enhanced survival at the lowest dietary Chol level.
Moulting of juvenile T. australiensis was initially similar for all dietary treatments over the first 2-3 weeks of the experiment, generally until after the first moult.At 4 weeks, subsequent moulting had already commenced for some lobsters in dietary treatments with ≥ 0.2% DM dietary Chol, seemingly accounting for slight differences in average wet weight of lobsters between 0% and ≥ 0.2% DM dietary Chol at 4 weeks.Over the remainder of the experiment, moulting slowed dramatically at 0% DM dietary Chol but continued as expected at ≥ 0.2% DM dietary Chol.These observations are consistent with previous findings that dietary Chol can influence moult frequency, intermoult duration and development time in mud crab 13 , Chinese mitten crab, Eriocheir sinensis 15 and blue swimmer crab, Portunus pelagicus 12 .The moult cycle is a fundamental aspect of crustacean biology that is intimately linked with metamorphosis, growth and reproduction 30,[34][35][36] .Since Chol is the principal precursor for the ecdysteroid moult hormones 4 , dietary Chol is expected to play an essential role in the regulation of moulting.
Survival was also significantly affected at 0% DM Chol with most mortalities occurring after the first moult.However, survival was significantly improved at 0% DM dietary Chol (45.83 ± 8.33%) when combined with 1% DM dietary PhosL (70.83 ± 11.02%).Studies have shown that insufficient dietary Chol can negatively affect survival and has been linked to a condition termed 'moult death syndrome' (incomplete ecdysis) in homarid lobsters Homarus sp. 37, crayfish Pacifastacus leniusculus 16 and crabs 12 .The present study similarly demonstrated that 0% DM dietary Chol disrupted the moult cycle of juvenile T. australiensis, although moult failure (incomplete ecdysis) was not observed, and in turn affected growth and survival rates.Since effects generally did not manifest at 0% DM dietary Chol until after the first moult, there is an implied connection between dietary intake/ availability and changes in nutritional condition over time.
Experimental feed Chol measured by GC-MS closely matched the target inclusion amounts of 0.2 and 0.4% DM, while a trace amount of dietary Chol of approx.0.05% DM was measured in feeds without Chol supplementation (nominally 0% DM dietary Chol).It was clear that dietary Chol had highly significant effects on the growth of juvenile T. australiensis.There was no difference in growth responses between 0.2 and 0.4% DM dietary Chol or between 0 and 1% DM dietary PhosL at any dietary Chol amount.However, after 8 weeks overall growth responses were approximately two-to threefold greater at ≥ 0.2% DM dietary Chol compared to 0% DM dietary Chol.Furthermore, comparable feeding and growth was observed for all treatments through the first moult of the experiment, after which feeding reduced, and growth plateaued or decreased in lobsters at 0% DM dietary Chol.Therefore, the poor growth observed at 0% DM dietary Chol was related to differences in both AFI and feed utilisation and, in accordance with FCR, it was observed that the 0% DM dietary Chol juveniles effectively consumed more feed per unit of growth.The poor growth of juvenile lobsters at 0% DM dietary Chol meant that, in absolute terms, AFI was significantly lower than the 0.2 and 0.4% DM Chol supplemented treatments.The lower growth at 0% DM dietary Chol in relation to FCR and AFI lead us to conclude that these effects were driven by Chol deficiency and resulting disruptions in normal behaviour and/ or physiological processes (e.g.moulting).
Growth at ≥ 0.2% DM dietary Chol was comparable with recent studies using 0.5% DM supplemental Chol in experimental feed formulations, where much higher total sterols were also measured (up to 1.5% DM), and T. australiensis lobsters of similar juvenile stage and experimental duration 28,32 .The apparent Chol requirement for growth of juvenile T. australiensis is relatively consistent with that for other decapod crustaceans.For penaeid shrimp, dietary Chol requirements have been reported to vary between 0.2 and 2.1% 2 .This range is skewed at the higher end by the results of Deshimaru and Kuroki 38 for the kuruma prawn, Marsupenaeus japonicus, although other early studies with this species also report wide-ranging optima of 0.2% to 1.0% supplemental Chol for larval and juvenile life stages [39][40][41] .Teshima et al. 42 later refined the requirement for juvenile kuruma prawn to between approx.0.29 and 0.60% actual Chol in the diet.Studies involving other species also report Chol requirements for optimal growth to be low, typically around ≤ 0.5% of the diet.For juvenile black tiger shrimp, Penaeus monodon, Chen 8 reported optimum growth at 0.5% supplemental dietary Chol.Sheen et al. 43 observed maximal growth at 0.19% actual dietary Chol with no significant difference in growth rate up to 0.81% in the diet of juvenile P. monodon.In line with these findings, Smith et al. 44 determined the optimal supplemental Chol requirement for subadult P. monodon to be around 0.17% of the diet.Similar low Chol requirements have been found for the Pacific white shrimp, L. vannamei 23,26 .For Pacific white shrimp, the maximum growth rate of juveniles has been observed at 0.11% actual Chol in the diet with an optimum of 0.15% determined by regression analysis 26 .Similar findings have been made for the American lobster, H. americanus, where supplemental Chol requirements have been reported in the range of 0.12-0.25%for larval and juvenile stages 18,21 ) with 0.5% achieving best growth rates in juveniles in another study 20 .For redclaw crayfish, Cherax quadricarinatus, an optimum of 0.49% actual dietary Chol was found 17 .Sheen 13 determined an optimum of 0.51% dietary Chol by regression analysis in juvenile mud crab, Scylla serrata.Irvin et al. 22 could not determine a dietary Chol requirement for juvenile tropical rock lobster, Panulirus ornatus, but suggested it was less than 0.125% of the diet.
Differences in Chol requirements between studies might be in part due to the presence of other sterols in feeds and the ability of certain species to effectively utilise these compounds 6,9,26 .In the present study, total sterols determined by TLC-FID were at least twofold greater than actual Chol measured by GC-MS due to unidentified sterol compounds present in the feed basal ingredients.Furthermore, since the presence of these sterols did not result in adequate growth or survival in the absence of supplemental dietary Chol, this may indicate juvenile T. australiensis have a specific requirement for Chol and/ or limited ability to effectively utilise other sterols.This may not be surprising given the predominately carnivorous and specialised feeding habits of Thenus spp. 45,46.Dietary PhosLs have previously been associated with Chol 'sparing' in some species 3 .While dietary PhosL did have significant effects on AFI and FCR, significant effects on the standard growth endpoints were not directly observed in juvenile T. australiensis.This could be at least in part due to the range of dietary Chol and PhosL concentrations examined.For example, Gong et al. 23 found similar growth rates at 0.2 and 0.5% dietary Chol at  , %) supplemental dietary concentrations after 0, 4 and 8 weeks.Mean weights were calculated using individual lobster weights at weeks 0 and 8. Mean weights at week 4 were estimated from bulk weighing.Table 2.Chemical composition and lipid profiles calculated for the whole-body (mean ± SEM, n = 3) of juvenile Thenus australiensis at three cholesterol (Chol, %) and two phospholipid (PhosL, %) supplemental dietary concentrations after 8 weeks.TPL = combined phospholipids, sphingolipids, glycolipids, carotenoid pigments and residual non-lipid material.P value in bold indicate statistically significant difference (P < 0.05).Where a statistical main effect (Chol and PhosL) or interaction (Chol*PhosL) was observed, superscripts are used to denote homogenous data ranges (P > 0.05) for treatment means determined by Tukey's post-hoc analysis.n.s.not significant.DM dry matter, WW wet weight, CP crude protein, TL total lipid, GE gross energy, TAG triacylglycerol, ST total sterols, TPL total polar lipid.

DM (% WW) CP (% DM) TL (% DM) Ash (% DM) GE (MJ kg −1 DM) TAG (% TL) ST (% TL) TPL (% TL)
Chol level 0.0% www.nature.com/scientificreports/all PhosL concentrations ranging from 0 to 5% in juvenile Pacific white shrimp.In a second experiment targeting a much lower dietary Chol range, they then observed a strong interactive effect between Chol and PhosL.In the second experiment, the Chol requirement for growth in juvenile Pacific white shrimp decreased significantly as dietary PhosL was serially increased, such that the Chol requirements were 0.05%, 0.13%, 0.14% and 0.35% at 5%, 3%, 1.5% and 0% total PhosL, respectively.Given the observed PhosL effects on AFI and FCR, and interactive effect on lobster survival, similar findings to Gong et al. 23,47 may also be observed for juvenile T. australiensis if different dietary Chol and PhosL ranges are employed in future experimental research.Dietary Chol was the most significant factor in determining chemical composition and overall nutritional condition in juvenile T. australiensis.At ≥ 0.2% DM dietary Chol, whole-body composition was broadly consistent with that expected for juvenile T. australiensis over the moult 30 .However, at 0% DM dietary Chol, lobsters were found to be in poor nutritional condition at the end of the experiment, as indicated by lower whole-body CP, TL, GE and higher proportional ash content.Whole-body lipid class profiles also revealed significantly reduced TAG and higher proportional ST and TPL contents, driven almost entirely by effects on HPSI and HP lipid content.The overall Chol*PhosL interaction for TL, TAG and TPL content of the HP is not easily explained.When viewed alongside moulting data, minor differences might be associated with slight variations in moult stage and timing between treatments 30 .However, these relatively minor differences aside, the greatest differences in HP lipid content and composition were very clearly associated with 0% DM dietary Chol.Lipid and energy storage is particularly important in crustaceans to endure transient non-feeding stages 48,49 and the energy demanding metabolic processes associated with ecdysis 34,50,51 .Reduced feed intake and mass loss between weeks 4 and 8, after the first moult had been successfully completed, suggests that at 0% DM dietary Chol juvenile T. australiensis had become dependent on utilisation of tissues to meet metabolic requirements 52 and after 8 weeks had virtually exhausted their HP TAG energy reserves.This starvation-like state and apparent inability to successfully complete a second moult en masse likely intensified effects of dietary Chol deficiency on moulting and perhaps ultimately affected survival.Although survival was higher at 0% DM dietary Chol when combined with 1% DM dietary PhosL, whole-body composition was similar at both dietary PhosL levels and all surviving lobsters were in similarly poor nutritional condition at the conclusion of the experiment.Tail muscle chemical composition did not differ between dietary treatments except for GE content which was significantly lower at 0% DM dietary Chol.In Atlantic ghost crab, Ocypode quadrata, 15-d starvation was found to have different metabolic effects in the different tissues observed as HP lipolysis and β-oxidation, HP gluconeogenesis and muscle glycogenolysis with depletion of glycogen 53 .Therefore, reduced feed intake resulting in the requirement for muscle glycogen as energy offers one possible explanation for the lower GE content in the TM.Nevertheless, the lack of other significant differences suggests that TM chemical composition may not be a particularly useful indicator of nutritional condition for T. australiensis.Low CP and high ash content of the whole-body indicates that lobsters at 0% DM dietary Chol likely possessed reduced total muscle content.Musculosomatic index (MSI) has previously been Table 3.Chemical composition and lipid profiles in tail muscle tissue (mean ± SEM, n = 3) of juvenile Thenus australiensis at three cholesterol (Chol, %) and two phospholipid (PhosL, %) supplemental dietary concentrations after 8 weeks.TPL = combined phospholipids, sphingolipids, glycolipids, carotenoid pigments and residual non-lipid material.P value in bold indicate statistically significant difference (P < 0.05).Where a statistical main effect (Chol and PhosL) or interaction (Chol*PhosL) was observed, superscripts are used to denote homogenous data ranges (P > 0.05) for treatment means determined by Tukey's post-hoc analysis.n.s.= not significant; n.d.= not detected.and so in future MSI may be a more useful supporting indicator of nutritional condition in juvenile T. australiensis.
The lack of clear significant effects of dietary PhosL on juvenile T. australiensis growth endpoints, probable indirect effects from improved feed efficiency aside, is worthy of some further consideration.In general, dietary PhosLs are also regarded as essential nutrients for fish and crustaceans 27 , though this is not as well-established in the literature for crustaceans 28 .Recent research has shown that dietary phosphatidylcholine (PC) is probably not essential for later stage juvenile T. australiensis (juvenile instar J6 onwards) owing to an apparent capacity for endogenous biosynthesis far exceeding possible dietary uptake 28 .Earlier stage juveniles (juvenile instar J4 onwards) were selected for the current experiment on the assumption that PhosL biosynthetic capacity may improve during juvenile development and theoretically reduced lipid digestive and biosynthetic capacities in earlier juveniles might help to uncover dietary nutrient relationships 27,55 .Supplemental choline was also omitted from experimental feed formulations, previously administered at 0.6% DM choline chloride 28 , to further limit the potential involvement of endogenous PC biosynthesis during growth.However, there were still trace amounts of choline found in all feeds, primarily derived from ingredients in the basal mix (approx.0.25% DM) with an additional smaller contribution (approx.0.05%) from refined soy lecithin in the 1% DM PhosL supplemented feeds.Therefore, endogenous PC synthesis in the absence of supplemental dietary PhosL cannot be ruled out in this experiment as having a potential effect on dietary Chol uptake and mobilisation.However, Gong et al. 47 previously did not observe an interaction between dietary Chol and PC in juvenile Pacific white shrimp, indicating that Chol 'sparing' in this species may be associated with PhosL's other than PC 23 .Despite the inclusion of mixed PhosL's in the form of refined soy lecithin, 1% DM supplemental PhosL resulted in fewer effects on overall growth performance compared to dietary Chol alone in the present study, potentially providing additional evidence that dietary PhosL requirements may be relatively low for juvenile T. australiensis 28 .However, inclusion of 1% DM supplemental dietary PhosL did have a significant beneficial effect on feed intake and feed conversion whereby less feed was consumed for each dietary Chol whilst achieving equivalent growth rates.Dietary PhosL at 1% DM also significantly improved lobster survival at the lowest dietary Chol level of 0% DM.Together these findings demonstrate that dietary PhosL had significant beneficial effects on nutrient uptake and/ or utilisation which may be expected given that dietary PhosL has been shown to support the mobilisation and transport of lipids from the gut into the haemolymph through Chol phospholipid lipoprotein complexes 37,[56][57][58][59][60][61][62] .Although dietary PhosL effects in this study were not as pronounced as those for dietary Chol, these effects are nonetheless important and may have particular value for practical feed development and commercial applications.

Conclusions
This study confirms that dietary Chol is essential for juvenile T. australiensis.After 8 weeks, lobsters fed 0% DM dietary Chol had significantly lower feed intake, moult frequency, growth, survival and nutritional condition compared to those at ≥ 0.2% DM dietary Chol.Cholesterol was the sole factor linked to differences in growth rates and whole-body chemical composition (condition) between 0% and ≥ 0.2% DM dietary Chol treatments, Table 4.Chemical composition and lipid profiles in hepatopancreas tissue (mean ± SEM, n = 3) of juvenile Thenus australiensis at three cholesterol (Chol, %) and two phospholipid (PhosL, %) supplemental dietary concentrations after 8 weeks.TPL = combined phospholipids, sphingolipids, glycolipids, carotenoid pigments and residual non-lipid material.P value in bold indicate statistically significant difference (P < 0.05).Where a statistical main effect (Chol and PhosL) or interaction (Chol*PhosL) was observed, superscripts are used to denote homogenous data ranges (P > 0.05) for treatment means determined by Tukey's post-hoc analysis..Post-hatchery juvenile slipper lobsters were cultured on fresh bivalve (Plebidonax deltoides) gonad until the third juvenile instar (J3) and then weaned onto a commercial-in-confidence nursery feed until intermoult J4 prior to experimentation.Upon commencement of the experiment, lobsters were individually weighed and then allocated to experimental aquaria based on size to ensure uniformity across all experimental treatment replicates (mean ± SD 4.50 ± 0.72 g, CV = 0.16).A total of 144 lobsters were stocked in 18 individual 18 L aquaria (0.38 m length × 0.24 m width × 0.25 m height) at a density of approx.88 lobsters m −2 (n = 8 lobsters per aquarium).At the time of stocking, an additional 8 lobsters were weighed (mean ± SD 4.13 ± 1.08 g, CV = 0.26), induced into a cold coma by emersion in a seawater ice slurry for 4-5 min, dissected and carcass remains/ tissues stored frozen at − 80 °C for baseline chemical composition 28,32 .Situated within a recirculating aquaculture system (RAS), all experimental aquaria were supplied with filtered, ozonated seawater at 27 °C at a rate of 6 exchanges h −1 and maintained under a 12:12 h blue light: dark photoperiod.Water quality (dissolved oxygen, salinity, pH, ORP and temperature) was monitored and recorded daily.

Experimental feeds
Six experimental feeds (Table 5), using a commercial-in-confidence basal mix, were prepared using three supplemental Chol concentrations of 0, 0.2 and 0.4% DM at two different supplemental phospholipid concentrations of 0 and 1.0% DM.To minimise potential spoilage and maintain freshness, experimental feeds were produced fortnightly using freshly prepared basal mix.Each feed was prepared by weighing out the required amount of fixed dry ingredient comprising the basal mix into a bowl.Lipid ingredients (fish oil, refined soy lecithin and Chol) were individually weighed out and combined to form a homogeneous lipid mixture.The lipid mixture was then slowly added to the basal mix and blended to a homogeneous semi-dry mash.The required water content was then added to the mash prior to feed manufacture.Details of the feed manufacturing method are commercial-in-confidence.After feed manufacture, a subsample (approx.6 g fresh weight) was collected from each batch of fresh, dried feed (n = 4 per feed) and stored frozen at − 20 °C pending chemical analysis (Table 6).Working feeds were stored at 4 °C in sealed, air-tight containers between fortnightly feed production batches, after which remaining feeds were discarded.
Justification of the chosen experimental feed lipid ingredient type and levels is provided as follows.In general, ingredient supplement levels were chosen based on previous similar works for other crustacean species 5,22,23,47,66 .As already described, Chol requirements for a broad range of decapod species has been found to be relatively low, generally ≤ 0.5% of the diet, and higher inclusion levels of > 0.8% DM can lead to negative effects in some species.However, Chol essentiality has not previously been established for any scyllarid or palinurid lobsters.Previous experimental studies on juvenile T. australiensis have employed experimental feeds with 0.5% DM supplemental Chol and measured total sterol levels ranging from 0.59 to 1.50% DM, without obvious negative effects or nutritional deficiencies being observed between feed treatments and experiments 28,32 .Landman et al. 32 also included a natural, fresh feed treatment of blue mussel (Mytilus galloprovincialis) possessing approx.0.9% DM total sterols.Within the related palinurid lobsters, Irvin et al. 22 attempted to determine dietary Chol requirements for juvenile tropical rock lobsters (Panulirus ornatus) but were unable to confirm essentiality or a definitive requirement in the absence of differing dietary Chol effects between 0.125 and 0.425% DM.For these reasons, supplemental Chol inclusion percentages of 0, 0.2 and 0.4% DM were selected for the current experiment to examine dietary Chol essentiality in juvenile T. australienis.Research has also shown that dietary phosphatidylcholine (PC) is probably not essential for juvenile T. australiensis owing to an apparent capacity for endogenous biosynthesis far exceeding possible dietary uptake 28 .Similarly, Gong et al. 47 also did not observe an interaction between dietary Chol and PC in juvenile Pacific white shrimp, indicating that Chol 'sparing' in this species may be associated with PhosL's other than PC 23 .For these reasons, a mixed PhosL source from refined soy lecithin at inclusion percentages of 0% and 1.0% DM was chosen to explore possible interactions of dietary PhosL and Chol in case other dietary PhosLs are also functionally more important than PC in juvenile T. australiensis.To mitigate potential effects of fatty acid composition from the plant based PhosL source (soy lecithin), an ultra-pure marine fish oil was selected to balance the total lipid content of feeds (isolipidic) and the ensure provision of essential fatty acids.

Experimental design
This experiment employed a 3 × 2 factorial design using the six experimental feeds as described above.Triplicate feed treatments were randomly allocated to experimental aquaria with the experiment conducted over eight consecutive weeks.The feeding protocol is described in the following section.Survival and moulting were monitored and recorded daily.Mortalities and exuvia were removed and visually inspected twice daily for evidence of disease or cannibalism.On completion of the experiment, surviving lobsters (total n = 117) were anaesthetised by submerging in a slurry of ice and seawater for 4-5 min.Each lobster was then individually blotted dry by paper towel before recording weight, carapace width and length measurements 30 .Each lobster was carefully dissected to remove the whole hepatopancreas (HP) and approximately 2 × 1 cm (length × width) strips of tail muscle (TM) tissue.Tissue samples were weighed for HPSI and subsequent biochemistry calculations.Following measurement and dissection, the carcass remains, HP and TM tissue samples were individually stored frozen at − 80 °C in preparation for freeze-drying and chemical analysis.Tail muscle, HP and carcass remains were analysed separately and the combined results used to calculate whole-body composition.

Feeding protocol and apparent feed intake
Experimental feeds were supplied in excess of requirements continuously over 16 h day −1 (approximately 1700 to 0900 h daily) using belt feeders, with a daily ration of approx.1.5% of body weight on a feed dry weight: lobster wet weight basis.Belt feeders were loaded once per day with a pre-weighed ration of feed derived from the initial total lobster biomass in each aquarium.At the mid-point of the experiment (4 weeks), a bulk-weighing (total wet weight of lobsters per aquarium) was performed to adjust feed rations relative to biomass changes due to growth and to mortality.Uneaten feeds were collected daily for determination of apparent feed intake (AFI), and each aquarium was cleaned by siphon before the subsequent feed period.Apparent feed intake was measured in situ as previously described 28,32 .Uneaten feed was collected on a 125 µm mesh screen, rinsed with deionised water to remove salts, weighed and stored frozen at − 20 °C in a cumulative weekly sample.Dry matter content of weekly uneaten feed composite samples (n = 3 per feed treatment per week) was subsequently determined after oven drying at 105 °C for 24 h 67 for input into daily AFI calculations.To correct AFI for feed DM losses, a feed leachability assessment was determined under the normal experimental conditions but in the absence of experimental lobsters.For the leachability assessment, a typical daily feed ration was delivered to each aquarium by belt feeder (n = 3 per feed treatment) over 16 h as during the experiment.Consistent with the daily experimental routine and timing, feeds were then removed from each aquarium by siphon, collected on a 125 µm mesh screen, rinsed with deionised water and oven dried at 105 °C for 24 h for DM determination.

Chemical composition analysis
Frozen samples were freeze-dried (FD) to a constant weight and then pooled by tissue/ sample type (experimental feeds, lobster carcass, HP and TM tissues) and treatment replicate.All FD samples were stored at − 80 °C prior to analysis.Dry matter content of FD samples was determined gravimetrically after oven drying at 105 °C for 24 h 67 .All biochemical analyses were performed on finely ground FD samples and corrected for DM.Ash content was determined by combustion of FD samples in a furnace at 600 °C for 2 h 68 .Crude protein content was determined after measuring elemental nitrogen (N) composition of FD samples using flash combustion isotope ratio mass spectrometry (Elementar vario PYRO cube coupled to an isoprime 100 mass spectrometer) at the Central Science Laboratory, University of Tasmania, Australia as described by Marchese et al. 69 .A conversion factor of 6.25 x %N was used to calculate crude protein (CP) content.Total lipid content of FD samples was determined gravimetrically using a modified Bligh and Dyer 70 method.Total lipid (TL) was extracted in a mixture of chloroform, methanol and milli-Q water (1:1:0.9v/v/v) as described by Yagiz et al. 71 .The total choline content of feeds was determined by Upscience Labs Solutions (https:// www.upsci ence-labs.com/ about-us/ our-world wide-prese nce/ vietn am/) according to in-house protocols.Bomb calorimetry was used to determine the gross energy (GE) content of FD samples according to manufacturer specifications (Parr 6400 Automatic Isoperibol Calorimeter, IL, USA).Table 5. Ingredient composition (% dry matter) of experimental feeds consisting of three cholesterol (Chol %) and two phospholipid (PhosL %) concentrations. 1 Basal mix-Commercial in confidence. 2 Ultralec® P Deoiled Lecithin-PhosL = 60% (Product 700851-ADM Australia Pty. Ltd). 3 From menhaden (Product F8020-Sigma Aldrich, Castle Hill, NSW, Australia). 4

Cholesterol determination
Quantitative Chol measurements were performed on aliquots of total lipid extracts (equivalent to approx.3 mg total lipid per sample).A surrogate standard of 10 µg D7-Chol (Cat.25265, Sapphire Biosciences Pty Ltd, Redfern, NSW, Australia) was added to each sample prior to saponification and extraction.Samples were evaporated to dryness at 35 °C under a stream of nitrogen gas.Total lipid extracts were saponified using 3 mL of 1% KOH in 80% methanol and heating for 3 h at 80 °C.Samples were cooled to room temperature, 1 mL milliQ water added and then mixed thoroughly.Extraction was performed in 1.5 mL of 4:1 (v/v) hexane: chloroform extraction solvent.Samples were mixed thoroughly, left to stand to allow phase separation and the upper phase then removed to a clean vial.The extraction step was repeated a further two times and the upper phase extracts combined.
Combined extracts were quantitatively transferred to GC vials and evaporated to dryness at 35 °C under a stream of nitrogen gas.Fifty microlitres of chloroform together with 50 µL of BSTFA (containing 1% TMCS) was added and samples heated at 60 °C overnight.Samples were then cooled, evaporated to dryness at 35 °C under a stream of nitrogen gas and made to 100 µL with chloroform.Cholesterol was analysed using a Varian CP-3800 gas chromatograph coupled to a Bruker 300MS triple quadrupole mass spectrometer (Bruker Corporation, Massachusetts, USA) fitted with an Agilent DB-5MS column (30 m × 0.25 mm; 0.25 µm film thickness).Helium was used as the carrier gas with a flow rate of 1.2 mL min −1 .The Injector was set to 290 °C and the Transfer line to 290 °C.Samples were injected at 45 °C in split mode (10:1).After 1 min, the oven was programmed from 45 to 120 °C at 30 °C min −1 , then at 4 °C min −1 to 320 °C, which was held for 20 min.Injection volume was 1 µL.Electron ionisation mass spectra were recorded in full scan mode over the range (m/z) 40 to 600.Single ion monitoring (SIM) acquisitions were also used as the following: Chol-TMS (m/z) 329.6, 368.6, 458.4;D7-Chol-TMS (m/z) 336.6, 375.6, 465.6.Identity of Chol was confirmed by comparison to the stable isotope labelled surrogate standard and the NIST2017 Mass Spectral Library (National Institute of Standards and Technology, USA).Data was processed using MS Workstation Version 7.

Calculations and statistical analysis
All calculations were performed as previously described 28 .Normality and homogeneity of variance were assessed using suitable tests (e.g., Shapiro-Wilk's and Levene's tests).Proportional data were arcsine square root transformed prior to analysis.For other data, log 10 transformations were used as required.Statistical comparisons were made by two-way analysis of variance (ANOVA) using feed Chol and PhosL as factors.Where statistically significant effects were observed, Tukey's post-hoc analysis was performed to establish significant differences between means.All statistical analyses were performed using the jamovi project (2020) R GUI jamovi software (v1.6.23)(retrieved from https:// www.jamovi.org).The critical level of statistical significance for all tests was α = 0.05.Table 6.Chemical and lipid class composition data (mean ± SD, n = 2) for homogenised composite experimental feeds comprised of three cholesterol (Chol, %) and two phospholipid (PhosL, %) concentrations.Experimental feeds were subsampled fortnightly (n = 4) to reflect average feeds composition over the duration of the experiment and then analysed in duplicate.TPL = combined phospholipids, sphingolipids, glycolipids, carotenoid pigments and residual non-lipid material.DM dry matter, WW wet weight, CP crude protein, TL total lipid, NFE nitrogen free extract, GE gross energy, TAG triacylglycerol, ST total sterols, TPL total polar lipid. https://doi.org/10.1038/s41598-024-60367-1

Figure 1 .
Figure 1.Mean (± SEM, n = 6) wet weight (g) of juvenile T. australiensis at three cholesterol (Chol, %) supplemental dietary concentrations after 0, 4 and 8 weeks.Mean weights were calculated using individual lobster weights at weeks 0 and 8. Mean weights at week 4 were estimated from bulk weighing.

General growth Survival (%) Moults (count) Moult frequency (moults ind. −1 ) AFI (mg DM ind. −1 d −1 ) FCR (g feed g −1 dry WG)
63osL had a significant beneficial effect on feed efficiency (AFI and FCR) at each dietary Chol level.A significant interactive effect (Chol*PhosL) was also found for lobster survival, primarily whereby 1% DM dietary PhosL benefited survival at the lowest 0% DM dietary Chol level.This study confirms the essentiality of dietary Chol for juvenile T. australiensis, that actual dietary Chol requirements appear to be relatively low at ≤ 0.2% DM and that higher dietary Chol may not provide any additional benefit to direct growth or condition.However, juvenile T. australiensis may have a specific dietary requirement for Chol and/ or limited ability to effectively utilise other sterols.The findings of a generally low dietary Chol requirement coupled with improved feed efficiency linked to dietary PhosL have significant value for future commercial lobster farming for waste minimisation and potential economic sustainability.Lobster husbandry and experimental research was conducted within the general framework and principles of the Australian Code for the Care and Use of Animals for Scientific Purposes63.The University of Tasmania does not require Animal Ethics Committee approval for research conducted on crustaceans based on the Tasmanian Animal Welfare Act 1993 (https:// www.legis lation.tas.gov.au/view/ whole/ html/ infor ce/ curre nt/ act-1993-063), which stipulates that Animal Ethics Committee approval is required for animal research conducted on living, non-human vertebrates and cephalopods.Juvenile slipper lobsters (Thenus australiensis) were reared from egg at the University of Tasmania, Institute for Marine and Antarctic Studies (IMAS), in February 2021 according to previously established protocols for tropical rock lobsters ≥ 99% Chol (Product C8667, Sigma Aldrich, Castle Hill, NSW, Australia).Lipid class analysesAn aliquot of total lipid (10-20 mg in 1 mL chloroform) was spotted on Chromarods S-V and developed in hexane:diethylether:acetic acid (70:10:0.1 v/v/v) and dried for 10 min at 80 °C.After drying, pyrolysis of Chromarods were performed by an Iatroscan™ MK-5 thin-layer chromatography-flame ionization detector analyser (Mitsubishi Kagaku Iatron, Inc., Japan).Peak areas were quantified by SIC-480II for Iatroscan™ Integrating Software v.7.0-E (System Instruments Co., Mitsubishi Chemical Medience Corporation, Japan).Lipid class was identified by comparison with corresponding standards.